RNAIII-independent target gene control by the agr quorum-sensing system : insight into the evolution of virulence regulation in Staphylococcus aureus

Cell-density-dependent gene regulation by quorum-sensing systems has a crucial function in bacterial physiology and pathogenesis. We demonstrate here that the Staphylococcus aureus agr quorum-sensing regulon is divided into (1) control of metabolism and PSM cytolysin genes, which occurs independently of the small regulatory RNA RNAIII, and (2) RNAIII-dependent control of additional virulence genes. Remarkably, PSM expression was regulated by direct binding of the AgrA response regulator. Our findings suggest that quorum-sensing regulation of PSMs was established before wide-ranging control of virulence was added to the agr regulon, which likely occurred by development of the RNAIII-encoding region around the gene encoding the PSM delta-toxin. Moreover, the agr regulon in the community-associated methicillin-resistant S. aureus MW2 considerably differed from that previously determined using laboratory strains. By establishing a two-level model of quorum-sensing target gene regulation in S. aureus, our study gives important insight into the evolution of virulence control in this leading human pathogen.

Medienart:

E-Artikel

Erscheinungsjahr:

2008

Erschienen:

2008

Enthalten in:

Zur Gesamtaufnahme - volume:32

Enthalten in:

Molecular cell - 32(2008), 1 vom: 10. Okt., Seite 150-8

Sprache:

Englisch

Beteiligte Personen:

Queck, Shu Y [VerfasserIn]
Jameson-Lee, Max [VerfasserIn]
Villaruz, Amer E [VerfasserIn]
Bach, Thanh-Huy L [VerfasserIn]
Khan, Burhan A [VerfasserIn]
Sturdevant, Daniel E [VerfasserIn]
Ricklefs, Stacey M [VerfasserIn]
Li, Min [VerfasserIn]
Otto, Michael [VerfasserIn]

Links:

Volltext

Themen:

Agr protein, Staphylococcus aureus
Bacterial Proteins
Bacterial Toxins
DNA, Bacterial
Journal Article
RNA, Bacterial
RNAIII, Staphylococcus aureus
Research Support, N.I.H., Intramural
Trans-Activators

Anmerkungen:

Date Completed 12.11.2008

Date Revised 03.10.2019

published: Print

Citation Status MEDLINE

doi:

10.1016/j.molcel.2008.08.005

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM182991040